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H2A去泛素化:哺乳动物表观基因组学——拓展组蛋白H2A去泛素化酶在细胞生物学和生理学中的前沿领域

H2A-DUBbing the mammalian epigenome: expanding frontiers for histone H2A deubiquitinating enzymes in cell biology and physiology.

作者信息

Belle Jad I, Nijnik Anastasia

机构信息

Department of Physiology, McGill University, Canada; Complex Traits Group, McGill University, Canada.

Department of Physiology, McGill University, Canada; Complex Traits Group, McGill University, Canada.

出版信息

Int J Biochem Cell Biol. 2014 May;50:161-74. doi: 10.1016/j.biocel.2014.03.004. Epub 2014 Mar 16.

Abstract

Posttranslational modifications of histone H2A through the attachment of ubiquitin or poly-ubiquitin conjugates are common in mammalian genomes and play an important role in the regulation of chromatin structure, gene expression, and DNA repair. Histone H2A deubiquitinases (H2A-DUBs) are a group of structurally diverse enzymes that catalyze the removal ubiquitin from histone H2A. In this review we provide a concise summary of the mechanisms that mediate histone H2A ubiquitination in mammalian cells, and review our current knowledge of mammalian H2A-DUBs, their biochemical activities, and recent developments in our understanding of their functions in mammalian physiology.

摘要

通过连接泛素或多聚泛素共轭物对组蛋白H2A进行的翻译后修饰在哺乳动物基因组中很常见,并在染色质结构调节、基因表达和DNA修复中发挥重要作用。组蛋白H2A去泛素化酶(H2A-DUBs)是一组结构多样的酶,可催化从组蛋白H2A上去除泛素。在本综述中,我们简要总结了哺乳动物细胞中介导组蛋白H2A泛素化的机制,并回顾了我们目前对哺乳动物H2A-DUBs的认识、它们的生化活性以及我们对其在哺乳动物生理学中功能理解的最新进展。

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